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骨髓移植后慢性移植物抗宿主病患者的非特异性抑制细胞

Nonspecific suppressor cells in patients with chronic graft-vs-host disease after marrow grafting.

作者信息

Tsoi M S, Storb R, Dobbs S, Kopecky K J, Santos E, Weiden P L, Thomas E D

出版信息

J Immunol. 1979 Nov;123(5):1970-6.

PMID:39962
Abstract

Forty-four human long-term survivors after marrow transplantation for aplastic anemia or hematologic malignancy were studied for the presence of circulating nonspecific suppressor cells. Twenty-two of the patients were healthy and 22 had mild to moderately severe chronic graft-vs-host disease (GVHD). Patient mononuclear cells (of donor origin) were tested for their ability to suppress the responses of lymphocytes obtained from the respective marrow donors to alloantigens in mixed leukocyte culture (MLC) and/or to concanavalin A (Con A). Tests were carried out between 199 and 2393 (median 376) days after transplantation. Cells from only 1 of 22 patients without chronic GVHD showed suppression of donor cell blastogeneis responses. In contrast, cells from 11 of 22 patients with chronic GVHD showed more than 30% suppression of donor cell responses in MLC and/or to Con A. The finding of suppressor cells was not related to the time of testing after grafting nor to immmunosuppressive therapy. Nonspecific suppressor activity was abrogated by irradiation with 1600 rads in vitro in five of six cases tested. Nonspecific suppressor cells may be one explanation for the severe combined immunodeficiency and the recurrent infectious complications characteristic of patients with chronic GVHD.

摘要

对44例因再生障碍性贫血或血液系统恶性肿瘤接受骨髓移植的人类长期存活者进行了循环非特异性抑制细胞的检测。其中22例患者健康,22例患有轻度至中度严重的慢性移植物抗宿主病(GVHD)。检测了患者(供体来源的)单核细胞抑制从各自骨髓供体获得的淋巴细胞在混合淋巴细胞培养(MLC)中对同种抗原和/或对刀豆球蛋白A(Con A)反应的能力。检测在移植后199至2393天(中位数376天)之间进行。22例无慢性GVHD的患者中只有1例的细胞显示出对供体细胞增殖反应的抑制。相比之下,22例患有慢性GVHD的患者中有11例的细胞在MLC中对供体细胞反应和/或对Con A的抑制超过30%。抑制细胞的发现与移植后检测时间无关,也与免疫抑制治疗无关。在六例检测的病例中,有五例体外经1600拉德照射后非特异性抑制活性被消除。非特异性抑制细胞可能是慢性GVHD患者严重联合免疫缺陷和反复感染并发症的一种解释。

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